ClinVar Miner

List of variants in gene MERTK reported as likely benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_006343.3(MERTK):c.844G>A (p.Ala282Thr) rs7588635 0.04692
NM_006343.3(MERTK):c.60A>T (p.Arg20Ser) rs35898499 0.03355
NM_006343.3(MERTK):c.-34G>A rs141412373 0.01554
NM_006343.3(MERTK):c.102A>G (p.Leu34=) rs143215350 0.00763
NM_006343.3(MERTK):c.1353A>G (p.Gln451=) rs35981104 0.00693
NM_006343.3(MERTK):c.*85dup rs147500027
NM_006343.3(MERTK):c.756A>G (p.Pro252=) rs3761702

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.